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Other Targets

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Cat. No. Product Name Field of Application Chemical Structure
DC21224 NMT1 inhibitor B13 NMT1 inhibitor B13 (LCL4) is a myristoylCoA analog that acts as a small molecule inhibitor of NMT1 with IC50 of 77.6 uM, blocks Src myristoylation and Src localization to the cytoplasmic membrane.
DC21391 NNC 05-2090 hydrochloride Featured NNC 05-2090 is a potent selective GABA transporter inhibitor of mGAT2 with Ki of 1.4 uM.
DC22893 NNC-0640 NNC-0640 (NNC 0640, NNC0640) is a potent, selective glucagon receptor (GCGR) negative allosteric modulator with IC50 of 69.2 nM.
DC21392 NNC-711 Featured NNC-711 is a potent and selective inhibitor of GABA uptake by GAT-1 with IC50 of 0.04 uM.
DC4204 Nocodazole Featured Nocodazole inhibits Abl, Abl(E255K) and Abl(T315I) with IC50 of 0.21 μM, 0.53 μM and 0.64 μM, respectively. Enhances homology-directed repair (HDR) efficiency 9 to 31% (depending on cell cycle phase) and increases Cas9-mediated gene editing frequencies.
DC4111 Nolatrexed (AG-337) Featured Nolatrexed (AG-337), inhibits purified recombinant human thymidylate synthase (TS) with a Ki of 11 nM, and displays non-competitive inhibition kinetics. It was further shown to inhibit cell growth in a panel of cell lines of murine and human origin, displ
DC10549 Nomifensine maleate Featured Nomifensine maleate is a selective inhibitor of dopamine uptake, used in adult attention deficit disorder.
DC9342 Noopept Noopept (GVS-111) is a medication promoted and prescribed in Russia and neighbouring countries as a nootropic.
DCAPI1558 Oxiracetam Nootropic agent shown to exhibit learning and memory improvement and cognitive function impairment prevention. Mechanism of action has not been quantified, but current theories suggest a modulation of glutamatergic and cholinergic neurotransmissions with
DC8848 Nosiheptide Nosiheptide is a bicyclic thiopeptide antibiotic produced by several species of actinomycetes, notably Streptomyces.
DC26002 TOPK inhibitor-1 Featured Novel PDZ binding kinase (PBK) inhibitor.
DC26003 (R)-9-(4-(1-(dimethylamino)propan-2-yl)phenyl)-8-hydroxythieno[2,3-c]quinolin-4(5H)-one Hydrochloride Featured Novel PDZ binding kinase (PBK) inhibitor.
DC10453 NP-118809 Featured NP-118809 is a N-type calcium channel blocker.
DC11212 NP161 NP161 is a potent and selective inhibitor of extracellular TRX (Thioredoxin 1) in vitro with IC50 of 0.54 uM.
DC22179 NPD13668 NPD13668 (NPD-13668) is a chemical novel modulator of EZH2-mediated gene silencing, inhibits EZH2/PCR2 activity and decreases H3K27me3 levels.
DC22180 NPD8733 Featured NPD8733 (NPD-8733) is a small-molecule ligand of valosin-containing protein (VCP)/p97, binds to the D1 domain of VCP/p97.
DC8398 NPS-1034 Featured NPS-1034 is a dual Met/Axl inhibitor with IC50 of 48 nM and 10.3 nM, respectively.
DC21928 NPT 200-​11 Featured NPT200-11 is an orally bioavailable and brain penetrating alpha-synuclein (ASYN) misfolding and aggregation inhibitor.
DC21397 AI-1 Nrf2 acticatior AI-1 is a small-molecule inducer of the antioxidant response element (ARE) that activates and stabilizes Nrf2 by covalently modifying Keap1, activates an ARE-dependent luciferase reporter with an EC50 of 2.7 uM.
DC21398 AI-2 Nrf2 acticatior AI-2 is a small-molecule inducer of the antioxidant response element (ARE) that activates and stabilizes Nrf2 by covalently modifying Keap1.
DC20477 Nrf2 activator 16 Nrf2 activator 16 is a potent Keap1-Nrf2 and Keap1-p-p62 protein-protein interaction inhibitor with IC50 of 0.91 uM and 1.8 uM respectively.
DC21399 AEM1 Featured NRF2 inhibitor AEM1 is a specific small molecule inhibitor of Nrf2 transcriptional activity in cancer cells, shows no activity against a panel of >100 kinases (including isoforms of PI3K, AKT, and PKC).
DC20251 NRX-103094 Featured NRX-103094 is an enhancer of an E3 ligase-substrate interaction.
DC20254 NRX-103095 Featured NRX-103095 is an enhancer of an E3 ligase-substrate interaction.
DC20248 NRX-1532 Featured NRX-1532 is an enhancer of an E3 ligase-substrate interaction.
DC20249 NRX-1933 Featured NRX-1933 is an enhancer of an E3 ligase-substrate interaction.
DC20252 NRX-252114 Featured NRX-252114 is a potent enhancer of the interaction between β-catenin, and its cognate E3 ligase, SCFβ-TrCP. NRX-252114 enhances the binding of pSer33/S37A β-catenin peptide for β-TrCP with an EC50 of 6.5 nM and a Kd of 0.4 nM. NRX-252114 induces mutant β-catenin degradation.
DC20253 NRX-252262 Featured NRX-252262 is an enhancer of an E3 ligase-substrate interaction.
DC20250 NRX2663 Featured NRX-2663 is an enhancer of the interaction between β-catenin, and its cognate E3 ligase, SCFβ-TrCP. NRX-2663 enhances the binding of β-catenin peptide for β-TrCP with an EC50 of 22.9 µM and a Kd of 54.8 nM[1].
DC8783 NS 9283 Featured NS 9283 is a positive allosteric modulator of α4β2 receptor; increases the potency of Ach-evoked currents ~60 fold without effecting the maximum efficacy (HEK293-hα4β2 cells).

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